Dynarex Corporation
⚠️ Moderate Risk
FEI: 2431014 • Orangeburg, NY • UNITED STATES
FEI Number
2431014
Location
Orangeburg, NY
Country
UNITED STATESAddress
10 Glenshaw St, , Orangeburg, NY, United States
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
NO 510(K)
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/16/2023 | 62HAL99ANTI-MICROBIAL N.E.C. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 7/29/2022 | 56FYO14BACITRACIN, N.E.C. (PEPTIDES) | Division of Northern Border Imports (DNBI) | |
| 9/3/2021 | 62FDJ99ANTI-INFECTIVE, TOPICAL N.E.C. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 7/22/2021 | 62FAL34POVIDONE IODINE (ANTI-INFECTIVE, TOPICAL) | Division of Southeast Imports (DSEI) | |
| 8/4/2008 | 73CAOAIRWAY, ESOPHAGEAL (OBTURATOR) | 118NOT LISTED | Chicago District Office (CHI-DO) |
| 5/23/2008 | 73CAOAIRWAY, ESOPHAGEAL (OBTURATOR) | Chicago District Office (CHI-DO) |
Frequently Asked Questions
What is Dynarex Corporation's FDA import refusal history?
Dynarex Corporation (FEI: 2431014) has 6 FDA import refusal record(s) in our database, spanning from 5/23/2008 to 11/16/2023.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Dynarex Corporation's FEI number is 2431014.
What types of violations has Dynarex Corporation received?
Dynarex Corporation has been cited for 4 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Dynarex Corporation come from?
All FDA import refusal data for Dynarex Corporation is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.